Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mehrangiz Noora"'
Autor:
Seyed Mehdi Hashemi, Nourollah Ramroodi, Hamed Amiri Fard, Sahar Talebian, Maryam Haghighi Rohani, Mahnaz Rezaei, Mehrangiz Noora, Saeedeh Salimi
Publikováno v:
Medicina, Vol 55, Iss 2, p 47 (2019)
Background and Objective: Evidence indicates that genetic factors may be involved in the risk of ischemic stroke (IS). The aim of this study was to assess the effect of genetic polymorphisms located in exons or untranslated regions of MTHFR as well a
Externí odkaz:
https://doaj.org/article/31b28dc3da6f44beb4ccbc5e70a53df9
Autor:
Saeedeh Salimi, Seyed Mehdi Hashemi, Mahnaz Rezaei, Mehrangiz Noora, Maryam Haghighi Rohani, Sahar Talebian, Hamed Amiri Fard, Nourollah Ramroodi
Publikováno v:
Medicina, Vol 55, Iss 2, p 47 (2019)
Medicina; Volume 55; Issue 2; Pages: 47
Medicina
Volume 55
Issue 2
Medicina; Volume 55; Issue 2; Pages: 47
Medicina
Volume 55
Issue 2
Background and Objective: Evidence indicates that genetic factors may be involved in the risk of ischemic stroke (IS). The aim of this study was to assess the effect of genetic polymorphisms located in exons or untranslated regions of MTHFR as well a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78e60d9470ebe8763eb0e12c50220975
https://www.mdpi.com/1010-660X/55/2/47
https://www.mdpi.com/1010-660X/55/2/47
Autor:
Saeedeh Salimi, Mahnaz Rezaei, Zahra Zakeri, Anoosh Naghavi, Mahnaz Sandoughi, Sima Nabizadeh, Farzaneh Farajian-Mashhadi, Hossain Shahraki, Mohammadoo-Khorassani Milad, Mehrangiz Noora
Osteopontin (OPN) is a chemokine-like glycoprotein that has a prominent role in regulating inflammation and immunity. OPN polymorphisms and elevated OPN levels are associated with systemic lupus erythematosus (SLE) in several populations. The aim of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82af0d4683f311e6b08722d061376b21
https://europepmc.org/articles/PMC4774351/
https://europepmc.org/articles/PMC4774351/
Autor:
Alireza Nakhaee, Saeedeh Salimi, Azita Zadehvakili, Soroush Dabiri, Mehrangiz Noora, Mahnaz Rezaei, Ebrahim Miri-Moghaddam
Publikováno v:
Majallah-i taḥqīqāt-i ̒ulūm-i pizishkī-i Zāhidān, Vol 14, Iss 3, Pp 39-43 (2012)
Background: glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common genetic defects in the world, so that more than 400 million people in worldwide are affected with it, but its prevalence varies from 1-65% in different populations. Cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::1271ba7e4177a8f676f36c8aaeb3c5df
http://www.zjrms.ir/browse.php?a_id=940&sid=1&slc_lang=en
http://www.zjrms.ir/browse.php?a_id=940&sid=1&slc_lang=en
Publikováno v:
Archives of gynecology and obstetrics. 285(2)
Preeclampsia is an important disorder of pregnancy that carries a severe morbidity and mortality risk for both mother and fetus. A large number of studies have shown that abnormalities in nitric oxide synthesis may contribute to the development of pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea36b6fcf1ad0d97d734fb7f673aa061
https://pubmed.ncbi.nlm.nih.gov/21713426
https://pubmed.ncbi.nlm.nih.gov/21713426